Senior Clinical Research Associate - Oncology - East Coast - Remote

Worldwide Clinical Trials is a global, midsize CRO dedicated to advancing patient care through innovative and collaborative clinical research.

• Manage research activities at sites participating in Worldwide’s clinical research projects.
• Perform all stages of clinical studies, including site identification, study start‑up activities, contract and budget negotiations, site training, and compliance monitoring.
• Conduct study initiation visits (SIVs) and manage site activities during study maintenance.
• Ensure compliance with informed consent, safety reporting, and all regulatory requirements.

• Excellent interpersonal, oral, and written communication skills in English.
• Superior organizational skills with meticulous attention to detail.
• Ability to work independently with minimal supervision.
• Proficiency in Microsoft Office, CTMS, and EDC Systems.

• 5+ years of experience as a Clinical Research Associate.
• 4‑year university degree or Nursing Degree.
• Experience in Oncology is required.
• Candidates must reside on the East Coast, United States.
• Willingness to travel regionally.

Worldwide is an equal‑opportunity employer committed to diversity, inclusion, and the professional success of all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or any other class protected by applicable law.